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BONE PATHOLOGY

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BONE PATHOLOGY * * * * * * * * * * * * * * * * Osteoporotic vertebral body (right) shortened by compression fractures, compared with a normal vertebral body. – PowerPoint PPT presentation

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Title: BONE PATHOLOGY


1
BONE PATHOLOGY
2
The Skeletal System
  • Parts of the skeletal system
  • Bones (skeleton)
  • Joints
  • Cartilages
  • Ligaments (bone to bone)(tendonbone to muscle)
  • Divided into two divisions
  • Axial skeleton
  • Appendicular skeleton limbs and girdle
  • The skeleton has 206 bones

3
Functions of Bones
  • Support of the body
  • Protection of soft organs
  • Movement due to attached skeletal muscles
  • Storage of minerals and fats
  • Blood cell formation

4
Normal bone
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Types of Bone Cells
  • Osteocytes
  • Mature bone cells
  • Osteoblasts
  • Bone-forming cells
  • Osteoclasts
  • Bone-destroying cells
  • Break down bone matrix for remodeling and release
    of calcium
  • Bone remodeling is a process in which both
    osteoblasts and osteoclasts participate

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Bone Fractures
  • A break in a bone
  • Types of bone fractures
  • Closed (simple) fracture break that does not
    penetrate the skin
  • Open (compound) fracture broken bone penetrates
    through the skin
  • Bone fractures are treated by reduction and
    immobilization
  • Realignment of the bone

9
Stages in the Healing of a Bone Fracture
Slide 5.19
10
Stages in the Healing of a Bone Fracture
  • 1-Haematoma formation
  • 2-Fibrocartilage callus formation
  • 3-Boney callus formation
  • 4-Bone remodelling

Slide 5.19
11
Classification of Bone Pathology
  • Infectious Diseases of Bone
  • Developmental Disorders of Bone
  • Metabolic Disorders of Bone
  • Avascular Bone Necrosis (Osteonecrosis)
  • Pagets Disease of Bone
  • Tumors of Bone

12
Infectious Diseases of Bone
  1. Osteomyelitis
  2. Potts Disease

13
OSTEOMYELITIS
  • Definition
  • This is inflammation of bone and bone marrow

14
Classification
  • Bacterial osteomyelitis
  • Acute suppurative osteomyelitis
  • Acute haematogenous osteomyelitis
  • Acute non-haematogenous osteomyelitis
  • Chronic osteomyelitis
  • Chronic non-specific osteomyelitis
  • Chronic specific osteomyelitis ( TB Syphilis)

15
  • Non- bacterial osteomyelitis
  • Viral osteomyelitis
  • Sarcoidosis
  • Radiation osteomyelitis

16
ACUTE HAEMATOGENIUS OSTEOMYELITIS
  • Definition
  • Acute osteomyelitis is an inflammation of bone
    caused by an infecting organism

17
  • Haematogenous osteomyelitis is predominantly seen
    in children and involves the highly vascular long
    bones especially those of the lower limbs.
  • In adults, haematogenous spread is more common to
    the lumbar vertebral bodies than elsewhere.

18
Pathogenesis
  • The spread of infection is usually haematogenous.
  • 1-Among children the metaphysis of the long
    bones is the most common site, where blood flow
    slows in the sinusoids, allowing bacteria to
    adhere to the vascular membranes.
  • 2-Local trauma with skin penetration and seeding
    of organisms is another pathway.
  • 3-Localized trauma without skin penetration to
    the bone causing haematoma, vascular obstruction
    in the metaphyseal region and bacteraemia around
    the same time result in infection.

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Metapheseal blood sinsoids
21
Stages of disease
  • 1-Inflammation Initial inflammation with
    vascular congestion and increased intra-osseous
    pressure.
  • 2-Suppuration Pus within the bones forces its
    way through the Haversian system and forms a
    subperiosteal abscess in 2-3 days.

22
  • 3-Sequestrum Vascular obstruction and infective
    thrombus decrease or obstruct the periosteal and
    endosteal blood supply, causing bone necrosis and
    sequestrum formation in approximately 7 days.
  • 4-Involucrum This is new bone formation from the
    stripped surface of periosteum.
  • 5-Resolution or progression to complications
    With antibiotics and surgical treatment early in
    the course of disease, osteomyelitis resolves
    without any complications.

23
MP of acute osteomyelitis
Inflammation of bone
24
Acute osteomyelitis
25
Complications of osteomyelitis
  1. Pathological fracture
  2. Spread of infection eg. Arthritis (joint
    inflammation), myositis (muscle inflammation) or
    neuritis (nerve inflammation)
  3. Blood spread causing toxaemia septicaemia
  4. Chronic suppurative osteomyelitis including
    sequestrum formation and skin sinus formation
  5. Damage to the growth plate causing subsequent
    growth deformity

26
Pott's disease
  • Pott's disease is a presentation of extra
    pulmonary tuberculosis that affects the spine, a
    kind of tuberculous arthritis of the
    intervertebral joints.
  • The lower thoracic and upper lumbar vertebrae are
    the areas of the spine most often affected.

27
Potts Disease
28
Tuberculosis of the spine in an Egyptian mummy
29
Clinical presentation
  1. Back pain
  2. Fever
  3. Night sweating
  4. Anorexia
  5. Weight loss
  6. Spinal mass, sometimes associated with numbness,
    paraesthesia or muscle weakness of the legs

30
Diagnosis
  • Blood tests elevated erythrocyte sedimentation
    rate (ESR)
  • Tuberculin skin test
  • Radiographs of the spine
  • Bone scan
  • CT of the spine
  • Bone biopsy
  • MRI

31
Potts Disease X-ray
Potts Disease MRI
32
Complications
  • Vertebral collapse resulting in kyphosis
  • Spinal cord compression
  • Sinus formation
  • Paraplegia (called Pott's paraplegia)

33
Tuberculous in long bones
  • Commonly around the knee, affects metaphysis and
    epiphysis, rarely diaphysis
  • Well-defined lytic area

34
Tuberculous in long bones
35
Tuberculous arthritis
  • The hip and knee are the most commonly affected
    peripheral joints.
  • Characterized by joint space narrowing and
    erosions which may lead to extensive destruction
    of the articular cortex.

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37
HEREDITARY BONE DISORDERS
  1. Achondroplasia
  2. Osteogenesis imperfecta
  3. osteopetrosis

38
Achondroplasia
  • Clinically
  • Long bones are short and thick ? short
    extremities ? dwarfism
  • Cranial and vertebral bone spared ? relatively
    large head and trunk
  • Normal intelligence, life span and reproductive
    ability

39
Achondroplasia
40
Osteogenesis imperfecta
  • Generalized osteopenia brittle bones, resulting
    in recurrent fractures and skeletal deformity
  • Most patients have an abnormally thin sclera with
    blue hue

41
Osteogenesis imperfecta
Abnormally thin sclera with blue hue
42
  1. Laxity of joint ligments leads to hypermobilty
  2. Involvement of the bones of the inner and middle
    ear produces deafness
  3. Some patients have dentinogenesis imperfecta
    small, fragile and discolored teeth due to
    deficiency of dentin
  4. The skin may be abnormally thin and the skin is
    susceptible to easy bruising

43
Laxity of joint ligaments
Osteogenesis imperfecta
Brittle bones
44
Dentinogenesis imperfecta
45
Osteopetrosis
  • Marble bone
  • Hereditary defect leading to thick sclerotic
    bones

46
  • Pathology
  • -Increased bone density and thickening of bone
    cortex
  • -The thickened bones are brittle and fracture
    easily
  • X-ray findings
  • Symmetrically generalized osteosclerosis
  • Long bones may have broadened metaphyses,
    resulting in an "Erlenmeyer flask" deformity

47
Osteopetrosis X-ray findings
Osteosclerosis
Erlenmeyer flask shaped deformity
48
Metabolic Diseases of Bone
49
Osteoporosis
  • Refers to increased porosity of skeleton.
  • Osteoporotic bones
  • Thin and fragile and are susceptible to fracture.

50
Osteoporotic vertebral body
Normal Vertebral body
51
  • Occurs due to
  • Loss of organic bone matrix and minerals.
  • Resulting in
  • Decreased bone mass and density.
  • Decreased thickness of cortical and trabecular
    bone.

52
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53
Types of Osteoporosis
  • Localized e.g. disuse of a limb
  • Generalized involves entire skeleton.
  • Primary
  • Old age (Senile)
  • Estrogen deficiency (postmenopausal)
  • Secondary (due to underlying disease)
  • Cushings disease (Hypercortisolism)
  • Drugs (Heparin and Steroids)

54
Postmenopausal Osteoporosis
  • Due to estrogen deficiency
  • Estrogen deficiency ? increased resorption of
    bone by osteoclasts and decreased formation of
    bone by osteoblasts.

55
Genetic factors
Nutrition
Peak bone mass
Physical activity
  • Menopause
  • ? estrogen
  • ? osteoclast activity
  • Aging
  • ? activity of osteoblasts
  • ? physical activity

Osteoporosis
56
Clinical findings
  • Bone pain
  • Weight bearing bones predisposed to
  • Compression of vertebral bodies (most common)
  • Colles fracture of distal radius.
  • Fracture femoral neck.
  • Loss of height and kyphosis

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58
  • Diagnosis
  • Dual energy X ray absorptiometry (DEXA) to
    evaluate bone density.

59
Osteonecrosis (Avascular Necrosis)
60
Osteonecrosis (Avascular necrosis)
  • Ischemic infarction of bone bone marrow.
  • Causes of ischemia
  • Vascular interruption (fracture)
  • Corticosteroids (most common)
  • Sickle cell disease
  • Common sites include
  • Femoral head
  • Scaphoid bone.

61
Osteonecrosis
62
Osteonecrosis
63
PAGETS DISEASE
64
  • Definition
  • Localized disorder of bone
  • Due to Excessive bone resorption followed by
    disorganized bone replacement
  • Resulting in Thickened but weak bone that is
    susceptible to deformity and fracture

65
  • Stages of paget disease
  • Osteolytic osteoclastic activity predominates
  • Mixed ostelytic-osteoblastic
  • Osteosclerotic osteoblastic activity
    predominates " burnout stage"

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  • Etiology
  • Possible slow virus infection
  • Possible genetic predisposition

68
  • Clinical features
  • Asymptomatic in most cases
  • Bone pain and deformities
  • Fractures
  • Warmth of overlying skin due to hypervascularity

69
  • Forms of involvement
  • Monosteotic (15) involving one bone
  • Polyosteotic (85) involving multiple bones
  • Common sites include the skull, pelvis, femur and
    vertebrae

70
PATHOLOGY
  • Microscopically
  • Haphazard arrangement of cement lines, creating a
    mosaic pattern
  • Skull involvement
  • Increase head size
  • Foramina narrowing causes impingement of cranial
    nerves, often leading to deafness
  • Involvement of facial bones may produce a
    lion-like facies

71
  • X-rays
  • Bone enlargement with lytic and sclerotic areas
  • Lab investigation
  • Highly elevated serum alkaline phosphatase
  • Complication
  • Osteosarcoma
  • Others sarcomas

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Osteolytic changes of the skull
74
Mosaic pattern of lamellar bone
75
BONE TUMORS
  • BENIGN TUMORS OF BONE

76
Classification of benign tumors of bone
  1. Osteoma
  2. Osteoid osteoma
  3. Osteoblastoma
  4. Osteochondroma
  5. Osteochondromatosis
  6. Enchondroma

77
Osteoma
  • Definition
  • Benign neoplasm that frequently involves the
    skull and facial bones

78
Osteoma
79
Osteoid osteoma
  • Definition
  • Benign, painful growth of the diaphysis of a long
    bone, often the tibia or femur
  • Clinically
  • Malesgt females
  • Age 5-25 years
  • Pain that is worse at night and relieved by
    aspirin
  • X-ray
  • Central radiolucency surrounded by sclerotic rim

80
Osteoid osteoma
81
Osteoblastoma
  • Similar to an osteoid osteoma but is larger
    (gt2cm) and often involves vertebrae

82
Osteochondroma (Exostosis)
  • Definition
  • Benign boney capped with cartilage that
    originates from epiphyseal growth plate
  • Clinical presentation
  • Adolescent males
  • Firm solitary growths at the end of the long
    bones
  • They may be asymptomatic or it causes pain,
    deformity or it can undergo malignant
    transformation (rare)

83
Osteochondroma
84
Osteochondroma
85
Osteochondromatosis
  • Multiple hereditary exostosis in which there is
    multiple symmetric osteochondromas

86
Enchondroma
  • Definition
  • Benign cartilaginous growth within the medullary
    cavity of bone, usually involving the hands and
    feet
  • Typically solitary and asymptomatic and require
    no treatment

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